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Lazic

FDA UDI

Class II (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name
LAZIC FDA UDI
Generic Name
Aneurysm clip FDA UDI
Device Name
Yasargil Titanium Clip STANDARD, temporary, 11mm slightly curved FDA UDI
Model / Reference
S.65.262 T FDA UDI
Description
Yasargil Titanium Clip STANDARD, temporary, 11mm slightly curved FDA UDI

Identifiers

Catalog Number
S.65.262 T FDA UDI
Primary DI / UDI-DI
04250603707783 FDA UDI
FDA Product Code
HCH FDA UDI
GMDN Term
Aneurysm clip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Aneurysm clip

Lazic by Peter Lazic GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneurysm clip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peter Lazic GmbH

Sources (1)

  • FDA UDI 90e58912-afb7-4a81-a7c0-79d70f77bbf7 35 fields · synced Jun 8, 2026